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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1989
[The effect of maternal dexamethasone treatment after the 12th week of pregnancy on fetal genital development in adrenogenital syndrome with 21-hydroxylase deficiency]K O Schwab, K Kruse, H G Dörr, et al.
The Journal of Pediatrics|January 15, 1998
Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidismK O Schwab, M Gerlich, M Broecker, et al.
Molecular Genetics and Metabolism|July 6, 2004
Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscleR Ensenauer, T Thiel, K O Schwab, et al.
BMC Medical Genetics|July 31, 2015
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screeningSarah C Grünert, A Wehrle, P Villavicencio-Lorini, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
Mutations of the TSH receptor as cause of congenital hyperthyroidismK O Schwab, P Söhlemann, M Gerlich, et al.
Journal of Diabetes Research|July 1, 2015
Overweight and Obesity Based on Four Reference Systems in 18,382 Paediatric Patients with Type 1 Diabetes from Germany and AustriaM Flechtner-Mors, K O Schwab, E E Fröhlich-Reiterer, et al.
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